A transparent thin film transistor device includes a transparent substrate, and a high dielectric constant insulator layer disposed over the transparent substrate at a defined temperature. A transparent semiconductor layer is disposed over the insulator layer.

Patent
   7541626
Priority
Mar 28 2005
Filed
Mar 28 2006
Issued
Jun 02 2009
Expiry
May 03 2027
Extension
401 days
Assg.orig
Entity
Small
5
10
EXPIRED
1. A transparent thin film transistor device comprising:
a transparent substrate;
a high dielectric constant insulator layer disposed over the transparent substrate at a defined temperature, said high dielectric constant insulator layer comprises at least one material selected from the group consisting of Bi2(Zn1/3Nb2/3)2O7, Bi1.5Zn1.0M1.5O7 (M=Nb, Ta, Sb), (Bi)1˜2(Zn, Nb, Ta, Ti)2O7, (Ca, Ba, Sr, Pb)1˜2(Zn, Nb, Ta, Ti, Zr)2O7, and (Ca1-xSrx)Bi4Ti4O15; and
a transparent semiconductor layer disposed over the high dielectric constant insulator layer.
13. A method of developing a transparent thin film transistor device comprising:
providing a transparent substrate;
forming a high dielectric constant insulator layer disposed over the transparent substrate at a defined temperature, said high dielectric constant insulator layer comprises at least one material selected from the group consisting of Bi2(Zn1/3Nb2/3)2O7, Bi1.5Zn1.0M1.5O7 (M=Nb, Ta, Sb), (Bi)1˜2(Zn, Nb, Ta, Ti)2O7, (Ca, Ba, Sr, Pb)1˜2(Zn, Nb, Ta, Ti, Zr)2O7, and (Ca1-xSrx)Bi4Ti4O15; and
forming a transparent semiconductor layer disposed over the high dielectric constant insulator layer.
2. The transistor device of claim 1, wherein the transparent substrate comprises glass, PET, PEN, PES, or Polyimide.
3. The transistor device of claim 1, wherein the high dielectric constant insulator layer is formed at least one process selected from the group consisting of sputtering, pulsed laser deposition, evaporation, chemical vapor deposition, and atomic layer deposition.
4. The transistor device of claim 1, wherein the high dielectric constant insulator layer is deposited at room temperature.
5. The transistor device of claim 1, wherein the high dielectric constant insulator layer is obtained below 300° C. deposition.
6. The transistor device of claim 1, wherein the high dielectric constant insulator layer is annealed in air or oxygen atmosphere below 300° C. following room temperature deposition.
7. The transistor device of claim 1, wherein the high dielectric constant insulator layer comprises a thickness no greater than approximately 2000 nm.
8. The transistor device of claim 1, wherein the high dielectric constant insulator layer comprises an amorphous or a nanocrystalline structure.
9. The transistor device of claim 1, wherein the high dielectric constant insulator layer comprises a high optical transmittance greater than 80%.
10. The transistor device of claim 1, wherein the high dielectric constant insulator layer comprises a capacitor structure for flexible embedded capacitor.
11. The transistor device of claim 1, wherein the transparent semiconductor layer comprises wide band gap oxide semiconductor where at least one material selected from the group consisting of ZnO, SnO2, In doped ZnO, and Ga doped ZnO.
12. The method of claim 1, wherein the transparent substrate comprises glass, PET, PEN, PES, or Polyimide.
14. The method of claim 13, wherein the high dielectric constant insulator layer is formed at least one process selected from the group consisting of sputtering, pulsed laser deposition, evaporation, chemical vapor deposition, and atomic layer deposition.
15. The method of claim 13, wherein the high dielectric constant insulator layer is deposited at room temperature.
16. The method of claim 13, wherein the high dielectric constant insulator layer is obtained below 300° C. deposition.
17. The method of claim 13, wherein the high dielectric constant insulator layer is annealed in air or oxygen atmosphere below 300° C. following room temperature deposition.
18. The method of claim 13, wherein the high dielectric constant insulator layer comprises a thickness no greater than approximately 2000 nm.
19. The method of claim 13, wherein the high dielectric constant insulator layer comprises an amorphous or a nanocrystalline structure.
20. The method of claim 13, wherein the high dielectric constant insulator layer comprises a high optical transmittance greater than 80%.
21. The method of claim 13, wherein the high dielectric constant insulator layer comprises a capacitor structure for flexible embedded capacitor.
22. The method of claim 13, wherein the transparent semiconductor comprises wide band gap oxide semiconductor where at least one material selected from the group consisting ZnO, SnO2, In doped ZnO, and Ga doped ZnO.

This application claims priority to provisional applications Ser. No. 60/665,672 filed Mar. 28, 2005, and Ser. No. 60/755,812 filed Jan. 3, 2006, both of which are incorporated herein by reference in their entireties.

The invention relates to the field of transistors, and in particular the fabrication of near room temperature processed high-K and low dielectric loss transparent transistor circuits using transparent high-K gate insulators.

Organic light emitting diodes (OLEDs) are of great interest due to their potential application in flat panel displays. More significantly, the hydrogenated amorphous silicon (a-Si:H) active matrix is a very promising technology for back-plane electronics for a new generation of displays based on OLEDs on transparent glass substrates. Amorphous Si has an advantage of lower processing costs despite its lower mobility compared to poly-Si.

Although there have been successful demonstrations of flexible OLED's fabricated on plastic substrates, the fabrication of a-Si transparent flexible transistor (TFT) on plastics has proven difficult due to mechanical and chemical instabilities of such substrates at the processing temperatures typically needed for a-Si transparent flexible transistor TFT (˜300° C.). For Active Matrix OLEDS (AMOLED) applications, SiNx gate dielectrics are commonly used for TFT fabrication. However the low dielectric constant of SiNx requires higher driver voltages, not compatible with battery powered wearable and portable devices. Currently, OLEDs can be made to emit light from bottom and top surfaces.

AMOLED displays have a transistor driver supplying a constant current source at each pixel with one switching TFT to program. Hence, AMOLED display pixels need a minimum of two TFTs to control the drive current. The transistor is used to separate the effect of the data line voltage and the address line voltage on the voltage across the OLED material. Each pixel with p-channel transistor is programmed to provide a constant current. Amorphous silicon and polycrystalline silicon are commonly used for AMOLEDs. Both of these materials are compatible with large area glass substrate processes, however, poly-Si technology is expensive compared to amorphous-Si technology even though poly-Si has much higher mobility. In terms of process temperature, amorphous-Si has an advantage. OLED display technology offers better viewing angles, more resolution and less power consumption than traditional LCD displays.

According to one aspect of the invention, there is provided a transparent thin film transistor device including a transparent substrate, and a high dielectric constant insulator layer disposed over the transparent substrate at a defined temperature. A transparent semiconductor layer is disposed over the insulator layer.

According to another aspect of the invention, there is provided a method of developing a transparent thin film transistor device. The method includes providing a transparent substrate, and forming a high dielectric constant insulator layer disposed over the transparent substrate at a defined temperature. Moreover, the method includes forming a transparent semiconductor layer disposed over the insulator layer.

FIG. 1 is a schematic diagram of an exemplary transparent flexible transistor (TFT) in accordance with the invention;

FIG. 2 illustrates an X-ray diffraction pattern for BZN thin films, showing only (222) peak of BZN film;

FIG. 3A is a graph showing the dielectric constant of BZN thin film (200 nm) as a function of annealing temperature; FIG. 3B is a graph showing the I-V characteristics of a BZN thin film as a function of annealing temperature;

FIG. 4 is a graph illustrating the optical transmittance of the indicated structures as a function of wavelength; and

FIG. 5A is a graph demonstration the drain-to-source current (IDS) as a function of drain-to-source voltage (VDS) at indicated gate-to-source voltages (VGS) of a ZnO TFT; FIG. 5B is a graph demonstration the log drain-to-source current (IDS) and square root of drain-to-source current (IDS) as a function of gate-to-source voltage (VGS) at drain-to-source voltage (VDS) of 4 V of a ZnO TFT.

The invention relates to forming high K-dielectrics Bi1.5Zn1.0Nb1.5O7 (BZN series, A2B2O7 structure materials) at room temperature and transparent transistors having transparent BZN thin films with high (>80%) optical transmittance. Specifically, one can demonstrate low voltage operating transparent flexible transistors (TFTs) performance by achieving relative dielectric constants of 50-55 and low leakage current density less than 10−7 A/cm2 at an applied voltage of 5 V. Also high dielectric constant and low dielectric loss at high frequency range makes room temperature processed BZN films applicable for thin film embedded capacitor

High-K gate oxides with high dielectric constant and low leakage current density can be used as a gate oxide to offer low voltage operation for a thin film transistor 2 (TFT), as shown in FIG. 1. The TFT 2 includes a transparent substrate 4, a source 10, a drain 12, an active channel 14, a gate oxide 6, and a gate 8. In this embodiment of the invention, the source 10 and drain 12 can comprise Al and the gate 8 can comprise Cr, however other similarly situated materials can be used for the source 10, drain 12, and gate 8. Note the gate 8 is totally surrounded by the gate oxide 6.

The invention proposes in-situ growth of a High-K gate oxide 6 to form TFTs, such as BZN films with amorphous structure, onto a transparent substrate 4 at reduced temperatures. For compatibility with a-Si TFT's, high-K oxide layer 6 growth can be achieved at 300˜400° C. with excellent low leakage characteristics. If required for compatibility with low cost polymer substrates, growth at or at or near room temperature is possible with some increase in leakage current. After the BZN growth, a semiconductor layer is, such as a-Si:H, poly-Si, p-channel pentacene semiconductor or n-channel semiconductor, is deposited on top of the high-K oxide layer 6 to form the active channel 14. The n-channel semiconductor can include ZnO or InGaO3. The transparent substrate 4 can include glass and plastic substrates from the following: PET, PEN, PES, Polyimide, or the like. Note the source 10 and drain 12 are formed on the active channel 14.

The high-K gate oxide layer 6 can include at least one material selected from the group consisting of Bi2(Zn1/3Nb2/3)2O7, Bi1.5Zn1.0M1.5O7 (M=Nb, Ta, Sb), (Bi)1˜2(Zn, Nb, Ta, Ti)2O7, (Ca, Ba, Sr, Pb)1˜2(Zn, Nb, Ta, Ti, Zr)2O7, and (Ca1-xSrx)Bi4Ti4O15. Also, the high-K gate oxide layer can be obtained at low temperatures (below 300° C.) deposition, and can be annealed in air or oxygen atmosphere (below 300° C.) following room temperature deposition. In addition, the high-K gate oxide layer can have a thickness no greater than approximately 2000 nm. Moreover, high-K gate oxide layer can be comprised of an amorphous, nanocrystalline structure or a capacitor structure for flexible embedded capacitors. The transparent semiconductor can include a wide band gap oxide semiconductor at least one material selected from the group consisting ZnO, SnO2, In doped ZnO, Ga doped ZnO.

Bismuth zinc niobate (Bi1.5Zn1.0Nb1.5O7, Bi2(Zn1/3Nb2/3)2O7, (Bi)1˜2(Zn, Nb, Ta, Ti)2O7) (BZN) with the pyrochlore structure has a high permittivity (˜170), low loss (<4×10−4), and high resistivity (˜3×1013 Ωcm). BZN has been studied for microwave tunable devices, and films can be grown by physical deposition methods (sputtering and pulsed laser deposition) or by chemical deposition (chemical vapor deposition, atomic layer deposition, sol-gel process).

The BZN films are formed at high temperature more than 500° C. and showed crystalline pyrochlore structure. Here, room temperature process is adapted to obtain amorphous structure with higher degree of order. The high dielectric constant achievable with BZN, even when processed at room temperature, can be explained in detail on the basis of its crystallographic structure. FIG. 2 illustrates the X-ray diffraction pattern for BZN thin films, showing only (222) peak of BZN film with higher degree of order. Thin film perovskite films like (Ba, Sr)TiO3 achieve good crystalline quality only at relatively elevated temperatures of around 600˜800° C. Also, The BZN films include a high optical transmittance greater than 80%.

On the other hand, BZN films, with the cubic pyrochlore structure, tend to achieve good crystalline quality at much lower temperatures (e.g. typically >400° C.). Indeed, perovskite materials often first form pyrochlore phases requiring subsequent elevated temperature annealing to achieve the equilibrium perovskite phase. Also, high sintering temperature around 1300˜1500° C. is required for perovskite phase like Pb(Zr, Ti)O3, (Ba, Sr)TiO3 etc. Also, BZN has cubic pyrochlore phase structure A2B2O7 which is relatively well formed at lower temperature compared to perovskite structure. Indeed, the peak intensities of BZN films are slightly stronger than those of room temperature deposited BST films pointing to a higher degree of order in BZN.

FIG. 3A shows dielectric constant of BZN thin film (200 nm) as a function of annealing temperature. The dielectric constant increased with increasing annealing temperature, from 51 at room temperature to 120 at 500° C. The increase is likely correlated with formation of the pyrochlore phase and increase in crystallinity and grain size for higher annealing temperatures. The inset in FIG. 3A shows the dielectric constant-frequency characteristics of Pt/BZN/Pt capacitors grown at room temperature.

The relative dielectric constant of the BZN thin film is nearly frequency independent, i.e. ˜55-51 in the frequency range between 103 and 106 Hz. MIM capacitor configuration showed low dielectric loss of 0.015 at 1 MHz. These represent potential application in plastic embedded capacitor. The high dielectric constant of these BZN films can be related to the ease with which the pyrochlore crystal structure forms at low temperature. This leads to a higher degree of short range order than that achieved by, e.g., perovskite-based oxides, and hence higher dielectric constants. Using BZN films, one can thus realize even lower operating voltages in OTFTs and thin film embedded capacitor.

FIG. 3B shows the I-V characteristics of a BZN thin film as a function of annealing temperature in a metal-insulator-metal (MIM) configuration utilizing Pt electrodes exhibiting excellent leakage current densities of less than 10−7 A/cm2 for voltages below 5 V. As increasing annealing temperature, leakage current density decreased until 400° C. After crystallization of BZN film at 500° C., leakage current density slightly increased. The leakage current density increased for the film annealed more than 600° C. The results may be related to reactions at the electrode interface or loss of volatile species such as Bi.

One can also demonstrate that amorphous or nanocrystalline BZN films, obtained by a number of means including a) room-temperature deposition and/or b) low temperature (below 300° C.) deposition or c) annealing (below 300° C.) following room temperature deposition, exhibit good dielectric and current leakage characteristics and serve as excellent candidates for use as a transistor gate-dielectric and a high-K oxide for thin film embedded capacitor, as shown in FIG. 2.

FIG. 4 shows the optical transmission spectra of the indicated structures containing the BZN film in the wavelength range between 200 and 900 nm. To investigate the transmittance of the BZN film, BZN/glass structures were examined. For comparison with the transmittance of ZnO films, tin-doped indium oxide (ITO) films, used as electrodes in transparent TFTs, were also investigated as a reference. Further, to isolate the relative contributions to the optical loss of the overall structure, the transmittance of the glass substrate, ZnO/glass, ZnO/BZN/glass, ITO/BZN/glass, and ITO/ZnO/BZN/glass structures were investigated.

The BZN/glass structure showed an absorption edge at 310 nm, which is shorter than that of the ZnO/glass structure (360 nm) but higher than that of the glass (280 nm). The transmittance at higher wavelengths than the absorption edge had oscillations due to interference effects. The average transmittance value was around 80% in all structures measured. The transmittance of the BZN film was better than or at least comparable to that of the ZnO and ITO films, indicating that transmission losses due to the BZN gate dielectric in TFTs would be negligible.

FIG. 5A shows the drain-to-source current (IDS) as a function of drain-to-source voltage (VDS) of the ZnO TFT with BZN gate insulator. The TFTs, normally off, operate via the accumulation of carries. The carriers are electrons and the channel is n-type given that IDS becomes nonzero for positive VGS. IDS at a VGS of 0 V is very small and the TFTs operates in the enhancement mode. The TFTs exhibited excellent current saturation with increasing VDS. The large output impedance, achieved at saturation, is desirable in most electronics applications.

FIG. 5B shows the transfer curve of the ZnO TFT. The threshold voltage (Vth) and field effect mobility (μFE) were calculated in the saturation region (VGS=4 V) from, respectively, the slope and x-axis intercept of the square root of IDS vs VGS plot. Vth and μFE were 2 V and 0.024 cm2/Vs, respectively. The subthreshold swing (SS) of the TFT was 0.25 V/dec. The device operated at a low voltage, below 4 V, due to the high gate capacitance. On-current and off-current at the operating voltage of 4 V were 0.3×10−6 A and 1.5×10−11, respectively giving an on/off current ratio of 2×104. While the TFT operated at low voltage (<4V), it had relatively low μFE and hence low on-current and on/off ratio

Room temperature processed high-K oxides with low dielectric loss and low leakage current density fabricated on plastic substrates or glass substrates can be used as TFT gate oxides to offer low voltage operation and insulator for embedded capacitor. AMOLED (active matrix organic light emitting diodes) displays have a transistor driver supplying a constant current source at each pixel with one switching TFTs to program. If one can fabricate transparent TFTs, bottom emissive structure will be realized.

Although the present invention has been shown and described with respect to several preferred embodiments thereof, various changes, omissions and additions to the form and detail thereof, may be made therein, without departing from the spirit and scope of the invention.

Tuller, Harry L., Kim, Il-Doo

Patent Priority Assignee Title
5882996, Oct 14 1997 Industrial Technology Research Institute Method of self-aligned dual damascene patterning using developer soluble arc interstitial layer
7855369, Nov 26 2007 SAMSUNG DISPLAY CO , LTD Radiation imaging element
7886436, Nov 07 2005 Samsung Electro-Mechanics Co., Ltd. Thin film capacitor-embedded printed circuit board and method of manufacturing the same
9520207, May 09 2014 The Penn State University; NATIONAL SCIENCE FOUNDATION Single phase lead-free cubic pyrochlore bismuth zinc niobate-based dielectric materials and processes for manufacture
9748019, May 09 2014 The Penn State Research Foundation Single phase lead-free cubic pyrochlore bismuth zinc niobate-based dielectric materials and processes for manufacture
Patent Priority Assignee Title
6207472, Mar 09 1999 GLOBALFOUNDRIES Inc Low temperature thin film transistor fabrication
6358378, Jan 26 2000 Korea Institute of Science and Technology Method for fabricating ZnO thin film for ultraviolet detection and emission source operated at room temperature, and apparatus therefor
6720119, Jul 27 2000 Fuji Xerox Co., Ltd. Method of fabricating high-dielectric color filter
6727522, Nov 17 1998 Japan Science and Technology Agency Transistor and semiconductor device
6878962, Mar 25 1999 Japan Science and Technology Agency Semiconductor device
20020060325,
20020086507,
20030218222,
20040056273,
20060115964,
///
Executed onAssignorAssigneeConveyanceFrameReelDoc
Mar 28 2006Massachusetts Institute of Technology(assignment on the face of the patent)
May 07 2006KIM, IL-DOOMassachusetts Institute of TechnologyASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0179880871 pdf
May 08 2006TULLER, HARRY L Massachusetts Institute of TechnologyASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0179880871 pdf
Date Maintenance Fee Events
Feb 03 2010ASPN: Payor Number Assigned.
Feb 03 2010RMPN: Payer Number De-assigned.
Dec 03 2012M2551: Payment of Maintenance Fee, 4th Yr, Small Entity.
Jan 13 2017REM: Maintenance Fee Reminder Mailed.
Jun 02 2017EXP: Patent Expired for Failure to Pay Maintenance Fees.


Date Maintenance Schedule
Jun 02 20124 years fee payment window open
Dec 02 20126 months grace period start (w surcharge)
Jun 02 2013patent expiry (for year 4)
Jun 02 20152 years to revive unintentionally abandoned end. (for year 4)
Jun 02 20168 years fee payment window open
Dec 02 20166 months grace period start (w surcharge)
Jun 02 2017patent expiry (for year 8)
Jun 02 20192 years to revive unintentionally abandoned end. (for year 8)
Jun 02 202012 years fee payment window open
Dec 02 20206 months grace period start (w surcharge)
Jun 02 2021patent expiry (for year 12)
Jun 02 20232 years to revive unintentionally abandoned end. (for year 12)